Labverity
Facility profile

SpecGx LLC

Testing & analysis · Drug product manufacturing · Hobart, NY

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed5 registered company locations
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisDistributeManufacturePackRelabelRepack
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
No action indicated (NAI)

Mar 13, 2020 · No conditions warranted FDA action in this inspection.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

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Shows

Registration status and a latest matched no action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

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Confirm the inspection scope and whether it covered the work you need.

Method and source details
View full inspection and compliance history7 inspection records

FDA inspection history

7 records, Jan 2010 – Mar 2020 · 3 NAI · 4 VAI · 0 OAI

DateClassProject areaCitationsFY
Mar 13, 2020NAIFood and Color Additives Petition Review2020
Mar 13, 2020NAIDrug Quality Assurance2020
Apr 6, 2018NAIDrug Quality Assurance2018
Jan 29, 2016VAIDrug Quality AssuranceYes2016
Aug 30, 2013VAIDrug Quality AssuranceYes2013
Apr 20, 2012VAIDrug Quality AssuranceYes2012
Jan 27, 2010VAIDrug Quality AssuranceYes2010

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

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